Endo Flashcards

1
Q
Serum Na – Low
UO - Normal or Low
Urine sodium – High
Intravascular vol status – Normal or high
Vasopressin Level – High
A

SIADH

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2
Q
Serum Na – Low
UO - High
Urine sodium – Very High
Intravascular vol status – Low
Vasopressin Level – Low
A

Cerebral Salt wasting

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3
Q
Serum Na – High
UO - High
Urine sodium – Low
Intravascular vol status – Low
Vasopressin Level – Low
A

Central DI

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4
Q

1 in 500-1,000 live male births; manifest as tall stature, learning disabilities, gynecomastia, dec U:L segment ratio; Boys: hypotonia, clinodactyly and hypertelorism; Testes small → indertility

A

(Klinefelter syndrome XXY syndrome)

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5
Q

Tall stature, severe acne in adolescence, inc incidence of learning disability; behavioral problems (impulsivity)

A

XYY syndrome

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6
Q

Thelarche

A

10-11 yr old

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7
Q

Pubarche

A

6-12 mo later

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8
Q

Menarche

A

2-2.5yr → 6 yr

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9
Q

Thinning of the scrotum

A

11-12 yr old

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10
Q

Axillary hair

A

mid-puberty

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11
Q

Treatment of D.I in neonates and young infants

A

Fluid therapy

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12
Q

Treatment of D.I in older Children

A

DDAVP (dosage: 25 – 300ug every 8-12 hr)

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13
Q

Polyuria and polydipsia with vasopressin deficiency

A

Central D.I

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14
Q

Polyuria and polydipsia with vasopressin insensitivity at the level of the kidney

A

Nephrogenic D.I

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15
Q

MC pituitary tumors in adolescent

A

Prolactin – secreting pituitary adenoma / Prolactinoma

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16
Q

Manifest as headache, primary or secondary amenorrhea, Galactorrhea

A

Prolactin – secreting pituitary adenoma / Prolactinoma

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17
Q

Prolactin level of mild Prolactin – secreting pituitary adenoma

A

40-50 ng/ml

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18
Q

Prolactin level of mild Prolactin – secreting pituitary adenoma

A

10,000-15,000 ng/ml

19
Q

Treatment for prolactinoma

A

Cabergoline

20
Q

Definitive diagnosis of GH deficiency

A

absent or low levels of GH in response to stimulation

21
Q

Definitive diagnosis of GH deficiency traditionally requires

A

Demonstration of absent or low levels of GH in response to stimulation

22
Q

DI manifest manifests clinically with

A

Polyuria and polydipsia and can result from either vasopressin deficiency or vasopressin insensitivity at the level of the kidney

23
Q

To differentiate central from nephrogenic DI, what test is needed

A

Water deprivation test

24
Q

Hyponatremia, inappropriately concentrated urine (>100 mOsm/kg), normal or slightly elevated plasma volume, normal to high urine sodium and low serum uric acid

A

SIADH

25
Q

Treatment of CSW

A

Consist of restoring intravascular volume with sodium chloride and water

26
Q

MC adenoma during childhood

A

Prolactinoma

27
Q

Central precocious puberty

A

breast development before the age of 8 yr in females and by the onset of testicular development before the age of 9 yr in males

28
Q

Most sensitive test for primary thyroid dysfunction

A

serum TSH

29
Q

Most cases of congenital hypothyroidism are caused by

A

Thyroid dysgenesis

30
Q

Most important method for identifying infants with congenital hypothyroidism

A

NBS

31
Q

Usually first clinical manifestation of acquired hypothyroidism

A

Slowing growth

32
Q

Typically preceded by a respiratory infection of pharyngitis, and the left lobe is more often affected. The infection may be caused by gram positive or gram negative organism, and abscess formation can occur

A

Acute infectious thyroiditis

33
Q

Most serious consequence of iodine deficiency and occurs only in geographic association with endemic goiter

A

Cretinism

34
Q

MC cause of endemic goiter worldwide

A

Iodine deficiency

35
Q

First line anti thyroid drug for children with Graves Disease

A

Methimazole

36
Q

Management goal of thyroid storm in adolescent

A

inhibition of thyroid hormone formation, sympathetic blockade and glucocorticoid therapy

37
Q

Principal regulators of calcium homeostasis

A

PTH and Vitamin D

38
Q

Acquired primary adrenal insufficiency is termed

A

Addison Disease

39
Q

More than 90% of CAH are caused by

A

21-hydroxylase deficiency

40
Q

The result of abnormally high blood levels of cortisol or other glucocorticoids. This can be iatrogenic or the result of endogenous cortisol secretion, a result of either an adrenal tumor or of hypersecretion of corticotropin by the pituitary or by a tumor

A

Cushing syndrome

41
Q

Hypertension in children is more often sustained rather than paroxysmal. When there are paroxysms of hypertension, the attacks are usually infrequent at first, but become more frequent and eventually give way to continuous hypertensive state. Between attacks of hypertension, the patient may be free of symptoms. During attacks, the patient complains of headache, palpitations, abdominal pain, dizziness, pallor nausea and sweating

A

Pheochromocytoma

42
Q

MC endocrine-metabolic disorder of childhood and adolescence, with important consequences for physical and emotional development

A

Hyperthyroidism

43
Q

Treatment for T1DM – Insulin
• Classification of DKA: Co2 = 10 – 15mEq/L venous, pH (venous) – 7.15 – 7.25 with Kussmaul respiration

A

Moderate

44
Q

Most important lifestyle factor association with development of T2DM

A

Obesity